An organic compound A `(C_(9)H_(10)O)` does not evolve any gas on reatement with Na-metal but on hydrolysis with dil. `H_(2)SO_(4)` gives `B(C_(9)H_(12)O_(2))` which on further treatement with alkaline solution of iodine gives an yellow precipitate. Also A on treatment with excess of conc. HBr gives `C(C_(9(H_(11)OBr)` as the major product. C on further treatment with `C_(2)H_(5)ONa//C_(2)H_(5)OH` followed by acidification of product gives D (an isomer of A). D on ozonolysis followed by work-up with dimethyl sulphide gives ortho hydroxyl benzaldehyde as one of the product. Answer the following three questions based on the above information. Which of the following statement regarding B is correct?A. B is an optically inactive substanceB. B is an optically active substance with same configuration as that of AC. B is an optically active substance with opposite configuration to that of A.D. A pure enantiomer of "A" will produce, on hydrolysis reaction, a racemic mixture of B